Dave had blood work done yesterday because they needed to see where his red/white cell counts were. If he was too low they were going to have to give him a blood transfusion. But, not the case. His counts are really good for someone who has had such a strong dose of Chemo. The 'Tiger in His Tank', according to Dave, is the Ambrotose that he has been faithfully taking since the onset of his condition. A friend of his recommended it for keeping the immune system strong and it does seem to be working. Kudos to Annie Ogden for getting him started on that. And Kudos to Dave for being such a good patient and taking it all the time.
More good news, he has driven himself to the Cancer Center for his injection a couple of times this week. That means he is feeling good.
Those Happy Thoughts Just Keep On Working,
Marilyn
Friday, August 31, 2007
Thursday, August 30, 2007
Cute Story
David and Kathy decided to have Olivia, Dave's youngest daughter, sleep over the other night. In the morning when it was time for breakfast, they made oatmeal. When Dave went to take a spoonful out of his bowl, Olivia, seeing that the oatmeal was very hot, decided to blow on her Papa's spoonful of oatmeal to cool it off for him so that he wouldn't burn his mouth. It really is the little things in life, isn't it.
Well, as of today, Dave has been told that he needs to wear a mask when he goes out to the Cancer Center for his injection. The high dose of Chemotherapy that he was given last Friday is about to do its job and knock his immune system down a few pegs. The Nupogen seems to be doing its work. Dave is in quite a lot of body pain, which means that the injections are encouraging his stem cells to proliferate. There is alot of pressure on the bones because the bone marrow is filling up. There will hopefully be some relief when the stem cells are harvested next week, but in the meantime, Percocet is working just fine. Just a few more days and he should be past this step and on to the next.
Happy thoughts are always welcome!!
Marilyn
Well, as of today, Dave has been told that he needs to wear a mask when he goes out to the Cancer Center for his injection. The high dose of Chemotherapy that he was given last Friday is about to do its job and knock his immune system down a few pegs. The Nupogen seems to be doing its work. Dave is in quite a lot of body pain, which means that the injections are encouraging his stem cells to proliferate. There is alot of pressure on the bones because the bone marrow is filling up. There will hopefully be some relief when the stem cells are harvested next week, but in the meantime, Percocet is working just fine. Just a few more days and he should be past this step and on to the next.
Happy thoughts are always welcome!!
Marilyn
Tuesday, August 28, 2007
He's Hanging In
It has been an up and down weekend for Dave. After Friday's Chemo, he felt okay until later in the evening and the next morning. He was experiencing fluid retention and some serious nausea, and being that it was Saturday, Kathy had an awful time getting in touch with someone to get a prescription for Lasix. Once she did, he started to feel a little better. Sunday was the first of eight Nupogen injections, which went well. As of this posting he has had two of these injections and so far, no side effects, although I'm told that he does carry a little bucket with him just in case his nausea decides to get eruptive.(giggle-giggle) So, for the most part, he seems to be doing well. He had such a great night last night that Kathy called Phyllis just to tell her how wonderful it was to see him feeling so good. Dave is one of the lucky ones who knows how to 'live' with cancer. He has a strong will, he can appreciate a good feeling (even for just a moment) and, most importantly, he has an angel by his side, who us mortals refer to as Kathy. If not for her determination, patience, and undying love and affection for this guy, his situation would be very different.
Thanks for your Happy Thoughts for Dave and Kathy!
Marilyn
Thanks for your Happy Thoughts for Dave and Kathy!
Marilyn
Friday, August 24, 2007
We'll Call This Day One.
According to his Mom, Day 1 has been half way decent for Dave. She stopped in to the Cancer Center this afternoon to see how he was doing and she said that he seemed fine. He was in and out of being sleepy and dizzy, but not much for nausea. That's one good thing. Kathy and Dave were at the Center from 9 am until about 6:30 pm. Very long day. (Of course the nurses over at the Cancer Center take very good care of them). So, he has tomorrow off and on Sunday he will start the
8 day Nupogen injections. (To make lots and lots of stem cells.)
This dose of Chemo that he had today will have knocked his immune system down quite a lot. They actually give him
an anti-biotic drip in between the Chemo. He needs to be very careful not to be around germs. Getting any kind of infection would just complicate things for him.
He is getting a lap top so that he can keep up with your messages and well wishes and funny stories, etc. while he is going through this. He should be able to use it while he is in the hospital, where he will check the Guest Book and the Blog frequently. (And be able to use e-mail).
That's pretty much it for now. If I get a chance to speak with Kathy on Saturday, I will update you.
Keep a Happy Thought,
marilyn
8 day Nupogen injections. (To make lots and lots of stem cells.)
This dose of Chemo that he had today will have knocked his immune system down quite a lot. They actually give him
an anti-biotic drip in between the Chemo. He needs to be very careful not to be around germs. Getting any kind of infection would just complicate things for him.
He is getting a lap top so that he can keep up with your messages and well wishes and funny stories, etc. while he is going through this. He should be able to use it while he is in the hospital, where he will check the Guest Book and the Blog frequently. (And be able to use e-mail).
That's pretty much it for now. If I get a chance to speak with Kathy on Saturday, I will update you.
Keep a Happy Thought,
marilyn
Thursday, August 23, 2007
He Is So Ready
I spoke with Dave today and he is ready for this thing. What a guy!! Tomorrow's Chemo treatment is an all day affair. It will be the first of three? very strong doses. (Hair loss is imminent with this type of Chemo.) I will let you know as soon as I do how he made out. Kudos to all of you who have posted such nice messages for our friend in his Guest Book. I know that he will read them again and again. Along with the many cards and letters that he continues to receive by mail. They really do make a difference.
Keep checking in.
Keep a happy thought for this dude.
Marilyn
Keep checking in.
Keep a happy thought for this dude.
Marilyn
Thursday, August 16, 2007
It's Only Just Begun...
Kathy and Dave and Ray had a very long day at Dana Farber on Wednesday. This is the beginning of the process for him. There are many tests that have to be taken before he starts on the 24th with the high dose of Chemotherapy. He managed, somehow, to emerge from the poking and proding, the 'man among men' that he is, I am told by his Mother. He remains very optimistic and in excellent spirits.
I would like to encourage you to go to the Guest Book and write a little something for Dave so that he has messages to read to give him some comfort during this procedure. Jim Doyle (who is becoming the 'Grand Master' of happy thoughts) has a little something to say about how we can help in other ways.
Also, I hope that you have all had a chance to read the latest Lion's Pride edition. If you don't get one, someone you know probably does. I will try to put it on the blog, Wendy Marshall-Hudzik, who is the 'Queen' of happy thoughts, wrote a lovely article (Class of 1970) about Dave's party and Barbara Maynard Scollan also wrote a nice article (Class of 1971). Dave was mentioned in the Hall of Fame section by his coach, Randy Whitehead, as well.
It truly is your love and friendship that keeps Dave optimistic. Let's not forget that we are on an important mission to see that he gets through this.
Thanks everyone!
Keep a Happy Thought!
Marilyn
I would like to encourage you to go to the Guest Book and write a little something for Dave so that he has messages to read to give him some comfort during this procedure. Jim Doyle (who is becoming the 'Grand Master' of happy thoughts) has a little something to say about how we can help in other ways.
Also, I hope that you have all had a chance to read the latest Lion's Pride edition. If you don't get one, someone you know probably does. I will try to put it on the blog, Wendy Marshall-Hudzik, who is the 'Queen' of happy thoughts, wrote a lovely article (Class of 1970) about Dave's party and Barbara Maynard Scollan also wrote a nice article (Class of 1971). Dave was mentioned in the Hall of Fame section by his coach, Randy Whitehead, as well.
It truly is your love and friendship that keeps Dave optimistic. Let's not forget that we are on an important mission to see that he gets through this.
Thanks everyone!
Keep a Happy Thought!
Marilyn
Sunday, August 12, 2007
Home Again, Home Again, Diggety Dog!
He just loves to be home! And finally on Wednesday night they let him go. I spoke with him today and he said that he is finally feeling better. Thursday, Friday and Saturday were not good days for him, but Sunday has turned out to be a beaute. His brother, Ray, was visiting when we spoke and Dave was his usual perky self. So, another carnival ride over, he's waiting in line for the next one.
'a happy thought is worth a thousand words '
Marilyn
'a happy thought is worth a thousand words '
Marilyn
Tuesday, August 7, 2007
Another Bump in the Road (maybe just a pimple!)
Dave was not feeling very well on Sunday, and he got so bad that Kathy took him over to the hospital, where he was admitted. He had a fever and was doing the shaky thing. Turns out it is just a minor infection. But as he is preparing for this stem cell procedure, nothing can be passed off as 'minor' to his medical team. So they have kept him in, as of tonite he has not been released. He is hoping to be going home on Wednesday. Kathy said that this should not affect the upcoming plans to start the stem cell process.
I would like to share with you all a conversation that I was fortunate enough to have today with a very nice young lady who told me that her uncle was diagnosed with end stage Multiple Myeloma at the age of 70. He also had a lot of bone damage, and she said that, aside from the year after the stem cell transplant, his last 7 years have been very good. The year after the transplant, he did experience a few respiratory infections. I was so encouraged by this story that I wanted to share it with all of you who are staying in the 'positive energy field' with regards to Dave and his situation.
So, lets keep yet another happy thought for the 'evacuation' of the infection, so that Dave can go home where he loves to be. I will keep you posted.
Marilyn
I would like to share with you all a conversation that I was fortunate enough to have today with a very nice young lady who told me that her uncle was diagnosed with end stage Multiple Myeloma at the age of 70. He also had a lot of bone damage, and she said that, aside from the year after the stem cell transplant, his last 7 years have been very good. The year after the transplant, he did experience a few respiratory infections. I was so encouraged by this story that I wanted to share it with all of you who are staying in the 'positive energy field' with regards to Dave and his situation.
So, lets keep yet another happy thought for the 'evacuation' of the infection, so that Dave can go home where he loves to be. I will keep you posted.
Marilyn
Friday, August 3, 2007
We Have Dates
Kathy and Dave have been in touch with the Docs and have set up the appointments to get the stem cell transplant started. There is quiite a lot involved and Dave is in pretty good spirits about it.
So, this is the schedule that Kathy gave me today:
Today was his last Chemo treatment at LGH. They want him to have a 3 week resting period. Rest from Chemo, not doctors. For the next 3 weeks they will be taking a ton of tests for all different kinds of things. They need to be sure that his body can handle this. Once he is cleared based on the tests, the procedure will officially begin on August 24th, starting with a very high dose of Chemotherapy that will be administered at LGH with Dr. Anamur. It's called 'mobilization Cytoxan'. I didn't find much about it when I looked it up. He has the 25th off, and on the 26th (and for the next 8 days) he will be given Nupogen injections, which, from what I understand, is the medication that produces stem cells and tricks them into entering the blood stream for easier collection (this procedure is done when a healthy host is donating bone marrow to someone else.) So, he has Labor Day off and for the following 4 days (9/4,5,6,&7) he will need to be at Dana Farber every morning at 7 am for what they call the 'harvesting' of his own stem cells. The doc's will actually take upwards of 5 million stem cells (amazing!) Kathy and Dave are on a housing list with Dana Farber so that they don't have to drive in every day. The
'harvesting' takes about 4-6 hours each time. September 8th is another day of rest, and then he enters Brigham and Women's hospital on the 9th. September 10th and 11th, he will be given the 'close to lethal' amount of Chemo. His immune system will be as non-functional as it can be after this dose. And then on the 12th, the stem cells will be re-infused.
He will remain in the hospital, under watchful care, until September 26th. That is the current release date. It's at this point that Dave needs to be extremely careful. He cannot be exposed to any kind of germ, bacteria, etc. Kathy said that the whole house has to be disinfected, (which luckily her Mom has already started), and he cannot be in the same room when someone is vacuuming. He will have to wear a mask when he goes out for at least the first 3 months. His immune system will remain very fragile for at least a year, though.
His food will have to be carefully monitored also. It's about as complicated as it gets, but it will help to give Dave a better and longer life.
His brother, Ray, is coming in tonite from Atlanta. He plans to stay for a few weeks and Dave is looking forward to spending some quality time with him.
Well, that's the schedule. Please try to use the Guestbook to send your messages to Dave. It would be beneficial to him if we could help keep his spirits up.
Thanks for your happy thoughts!
Marilyn
So, this is the schedule that Kathy gave me today:
Today was his last Chemo treatment at LGH. They want him to have a 3 week resting period. Rest from Chemo, not doctors. For the next 3 weeks they will be taking a ton of tests for all different kinds of things. They need to be sure that his body can handle this. Once he is cleared based on the tests, the procedure will officially begin on August 24th, starting with a very high dose of Chemotherapy that will be administered at LGH with Dr. Anamur. It's called 'mobilization Cytoxan'. I didn't find much about it when I looked it up. He has the 25th off, and on the 26th (and for the next 8 days) he will be given Nupogen injections, which, from what I understand, is the medication that produces stem cells and tricks them into entering the blood stream for easier collection (this procedure is done when a healthy host is donating bone marrow to someone else.) So, he has Labor Day off and for the following 4 days (9/4,5,6,&7) he will need to be at Dana Farber every morning at 7 am for what they call the 'harvesting' of his own stem cells. The doc's will actually take upwards of 5 million stem cells (amazing!) Kathy and Dave are on a housing list with Dana Farber so that they don't have to drive in every day. The
'harvesting' takes about 4-6 hours each time. September 8th is another day of rest, and then he enters Brigham and Women's hospital on the 9th. September 10th and 11th, he will be given the 'close to lethal' amount of Chemo. His immune system will be as non-functional as it can be after this dose. And then on the 12th, the stem cells will be re-infused.
He will remain in the hospital, under watchful care, until September 26th. That is the current release date. It's at this point that Dave needs to be extremely careful. He cannot be exposed to any kind of germ, bacteria, etc. Kathy said that the whole house has to be disinfected, (which luckily her Mom has already started), and he cannot be in the same room when someone is vacuuming. He will have to wear a mask when he goes out for at least the first 3 months. His immune system will remain very fragile for at least a year, though.
His food will have to be carefully monitored also. It's about as complicated as it gets, but it will help to give Dave a better and longer life.
His brother, Ray, is coming in tonite from Atlanta. He plans to stay for a few weeks and Dave is looking forward to spending some quality time with him.
Well, that's the schedule. Please try to use the Guestbook to send your messages to Dave. It would be beneficial to him if we could help keep his spirits up.
Thanks for your happy thoughts!
Marilyn
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